European Journal of Human Genetics

FIGURE 1

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Phenotypic and molecular characterisation of the Aarskog–Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients

Alfredo Orrico, Lucia Galli, Maria Luigia Cavaliere, Livia Garavelli, Jean-Pierre Fryns, Ellen Crushell, Maria Michela Rinaldi, Ana Medeira and Vincenzo Sorrentino

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Figure 1.

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Characteristic facial appearance of patient 53.

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